Department of Surgery, Okazaki City Hospital, Okazaki, Japan.
Department of Gastroenterological Surgery (Surgery II), Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan.
World J Surg. 2019 Aug;43(8):2016-2024. doi: 10.1007/s00268-019-04942-y.
Discontinuation of postoperative S-1 adjuvant monotherapy is a frequent problem in the management of patients with gastric cancer.
A total of 355 stage II/III gastric cancer patients who underwent gastrectomy and adjuvant S-1 were retrospectively analyzed using a multicenter dataset. We randomly assigned patients into either discovery or validation cohort in a 2:1 ratio. In the discovery cohort, 29 parameters were assessed as candidate factors to predict discontinuation of S-1 adjuvant within 6 months. A scoring system was designed using independent risk factors identified by the multivariate analysis. Reproducibility was tested in the validation cohort.
Overall, 92 patients (25.9%) discontinued the treatment within 6 months because of adverse effects. Age, preoperative urea nitrogen (UN) and the preoperative albumin-to-bilirubin index (ALBI) showed the highest area under the curve (AUC) for the discontinuation of S-1 adjuvant within 6 months in each category: body status, blood tests and indices. In the multivariate analysis, age ≥ 64 years, preoperative UN ≥ 15.2 mg/dl and preoperative ALBI ≥ -0.265 were identified as independent risk factors. A scoring scale consisting of these three factors was developed for the prediction of drug discontinuation and demonstrated a greater AUC (0.728) than that of each of the three constituents. The time to treatment discontinuation decreased incrementally as the risk score increased. The reproducible findings were confirmed in the validation cohort.
We identified risk factors and developed a scoring scale to predict S-1 adjuvant monotherapy discontinuation in patients with stage II/III gastric cancer.
术后 S-1 辅助单药治疗的停药是胃癌患者管理中的一个常见问题。
回顾性分析了接受胃切除术和辅助 S-1 治疗的 355 例 II/III 期胃癌患者的多中心数据集。我们将患者按 2:1 的比例随机分配到发现队列或验证队列。在发现队列中,评估了 29 个参数作为预测 S-1 辅助治疗 6 个月内停药的候选因素。使用多因素分析确定的独立危险因素设计评分系统。在验证队列中测试了可重复性。
总体而言,92 例(25.9%)患者因不良反应在 6 个月内停止治疗。年龄、术前尿素氮(UN)和术前白蛋白-胆红素指数(ALBI)在每个类别(身体状况、血液检查和指数)中对 S-1 辅助治疗 6 个月内停药的曲线下面积(AUC)最高。多因素分析显示,年龄≥64 岁、术前 UN≥15.2mg/dl 和术前 ALBI≥-0.265 是独立的危险因素。基于这三个因素开发了一个评分量表,用于预测药物停药,其 AUC(0.728)大于三个因素中的任何一个。随着风险评分的增加,治疗停药的时间逐渐减少。验证队列中也得到了可重复的结果。
我们确定了风险因素,并开发了一个评分系统,以预测 II/III 期胃癌患者 S-1 辅助单药治疗的停药。